PIPA: A phase Ib study of β-isoform sparing phosphatidylinositol 3-kinase (PI3K) inhibitor taselisib (T) plus palbociclib (P) and fulvestrant (FUL) in PIK3CA-mutant (mt) ER-positive and taselisib (T) plus palbociclib (P) in PIK3CA-mutant (mt) ER-negative advanced breast cancer.

Authors

null

Javier Pascual

Royal Marsden Hospital and The Institute of Cancer Research, London, United Kingdom

Javier Pascual , Iain R. MacPherson , Anne Caroline Armstrong , Sarah Emily Ward , Mona Parmar , Alison Joanne Turner , Hannah Bye , Paula Proszek , Andrew Dodson , Isaac Garcia-Murillas , Jenny King , Emma Hall , Laura Finneran , Juanita Suzanne Lopez , Alicia Frances Clare Okines , Alistair E. Ring , Nicholas C. Turner

Organizations

Royal Marsden Hospital and The Institute of Cancer Research, London, United Kingdom, Beatson West of Scotland Cancer Centre, Glasgow, United Kingdom, Christie Hospital NHS Foundation Trust, Manchester, United Kingdom, The Institute of Cancer Research, Sutton, United Kingdom, Institute of Cancer Research, London, United Kingdom, The Royal Marsden/Institute of Cancer Research, London, United Kingdom, Royal Marsden NHS Foundation Trust, London, United Kingdom, The Institute of Cancer Research, London, United Kingdom, Clinical Trials and Statistics Unit, The Institute of Cancer Research, London, United Kingdom, Drug Development Unit-The Institute of Cancer Research and The Royal Marsden NHS Foundation Trust, Sutton, United Kingdom, The Royal Marsden NHS Foundation Trust, London, United Kingdom, The Royal Marsden NHS Foundation Trust, Sutton, United Kingdom

Research Funding

Pharmaceutical/Biotech Company

Background: PI3K and CDK4/6 inhibitors synergise in ER+ve and –ve PIK3CA-mt breast cancer (BC) models. Escalation phase of this study set recommended phase 2 dose (RP2D) at P 125mg on a 3/1 scheme plus T 2mg daily (Lim, ASCO 2017). Here we present the results of expansion cohorts for PIK3CA-mt BC patients (pts). Methods: The primary objective was to assess the confirmed objective response rate (ORR) of the P + T + FUL triplet in pts with measurable PIK3CA-mt ER+ve HER2-ve advanced BC, with up to two prior lines of chemotherapy for advanced disease. PIK3CA mutation was assessed in tissue or plasma DNA analysis. Exploratory objectives included assessment of efficacy of P + T in a cohort of pts with PIK3CA-mt advanced ER-ve BC. Safety is reported overall for 44 patients including an additional cohort of 7 PIK3CA-unknown ER+ve BC pts treated with P + T + letrozole (LET). For the P + T + FUL triplet a Simon minmax design was used, with 6 responses in 25 patients required to declare efficacy. Results: We recruited 24 assessable patients with PIK3CA-mt ER+ve HER2-ve advanced BC, median age 57 (42-74), median 3 (1-9) prior therapy lines for advance disease, with 24 (100%) receiving prior endocrine therapy and 23 (96%) prior aromatase inhibitor. ORR was 33% (8/24, 95% CI 16-55%), with median progression free survival (PFS) 7.9m (95% CI 5.6-11.8). For the 11 assessable PIK3CA-mt ER-ve pts (8 HER2-ve, 3 HER2+ve) receiving P + T, ORR was 0% (0/11), clinical benefit rate (CBR) 27% (3/11) and median PFS 4.3m (95% CI 1.8-6.1). Most common AEs across all cohorts were neutropenia (80%), fatigue (50%), mucositis (50%) and thrombocytopenia (30%). Most common grade 3/4 AEs were neutropenia (57%) and rash (11%). Translational research is ongoing. Conclusions: The triplet of P + T + FUL has promising efficacy in pre-treated PIK3CA-mt ER+ve advanced BC. A subset of patients with PIK3CA-mt ER-ve advanced BC had clinical benefit from P + T. The combination of P + T +/- FUL/LET was well tolerated with anticipated AEs. Clinical trial information: NCT02389842

Disclaimer

This material on this page is ©2024 American Society of Clinical Oncology, all rights reserved. Licensing available upon request. For more information, please contact licensing@asco.org

Abstract Details

Meeting

2019 ASCO Annual Meeting

Session Type

Poster Session

Session Title

Breast Cancer—Metastatic

Track

Breast Cancer

Sub Track

Hormone Receptor-Positive

Clinical Trial Registration Number

NCT02389842

Citation

J Clin Oncol 37, 2019 (suppl; abstr 1051)

DOI

10.1200/JCO.2019.37.15_suppl.1051

Abstract #

1051

Poster Bd #

132

Abstract Disclosures